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Author Details

Andrew B Singleton
National Institute on Aging
1997
615
123
PMIDPaper TitleJournal TitlePublished Year
38066663Moving towards the detection of frailty with biomarkers: A population health study.Aging Cell2024
38066663Moving towards the detection of frailty with biomarkers: A population health study.Aging Cell2024
36669485Virus exposure and neurodegenerative disease risk across national biobanks.Neuron2023
37606627Artificial intelligence for dementia genetics and omics.Alzheimers Dement2023
38014237Human brain single nucleus cell type enrichments in neurodegenerative diseases.Res Sq2023
37729920A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline.Cell Rep Methods2023
37704671Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37611509Polygenic risk score for Parkinson's disease and olfaction among middle-aged to older women.Parkinsonism Relat Disord2023
37409055Application of Aligned-UMAP to longitudinal biomedical studies.Patterns (N Y)2023
37090536Analysis of rare Parkinson's disease variants in millions of people.Res Sq2023
37467655MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset.Parkinsonism Relat Disord2023
37024536Exploring the genetic and genomic connection underlying neurodegeneration with brain iron accumulation and the risk for Parkinson's disease.NPJ Parkinsons Dis2023
36774388A proteogenomic view of Parkinson's disease causality and heterogeneity.NPJ Parkinsons Dis2023
37334620Parkinson's Disease Case Ascertainment in the Sister Study: A Cohort for Environmental Health Research.J Parkinsons Dis2023
37398408Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.medRxiv2023
37398091Genome-wide meta-analysis of CSF biomarkers in Alzheimer's disease and Parkinson's disease cohorts.medRxiv2023
36950378The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism.Cell Genom2023
37198259Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease.Mol Psychiatry2023
37192343Genetic risk factor clustering within and across neurodegenerative diseases.Brain2023
36871034The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data.NPJ Parkinsons Dis2023
36695634Genome-Wide Analysis of Structural Variants in Parkinson Disease.Ann Neurol2023
37386035Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10.NPJ Parkinsons Dis2023
37369645Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
36993627<i>MAPT</i> allele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson's disease risk and age at onset.medRxiv2023
37425910Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System Atrophy.medRxiv2023
37168844Variant biomarker discovery using mass spectrometry-based proteogenomics.Front Aging2023
36854767LRRK2 and GBA1 variant carriers have higher urinary bis(monacylglycerol) phosphate concentrations in PPMI cohorts.NPJ Parkinsons Dis2023
37225742Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data.NPJ Parkinsons Dis2023
36788297Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers.Mov Disord2023
36669485Virus exposure and neurodegenerative disease risk across national biobanks.Neuron2023
37539664Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease Cohorts.Mov Disord2023
37163045Creating the Pick's disease International Consortium: Association study of <i>MAPT</i> H2 haplotype with risk of Pick's disease.medRxiv2023
38014237Human brain single nucleus cell type enrichments in neurodegenerative diseases.Res Sq2023
37704671Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37611509Polygenic risk score for Parkinson's disease and olfaction among middle-aged to older women.Parkinsonism Relat Disord2023
37606627Artificial intelligence for dementia genetics and omics.Alzheimers Dement2023
37539664Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease Cohorts.Mov Disord2023
37729920A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline.Cell Rep Methods2023
37425910Genome-wide association study identifies a new susceptibility locus in <i>PLA2G4C</i> for Multiple System Atrophy.medRxiv2023
37192343Genetic risk factor clustering within and across neurodegenerative diseases.Brain2023
37090536Analysis of rare Parkinson's disease variants in millions of people.Res Sq2023
37024536Exploring the genetic and genomic connection underlying neurodegeneration with brain iron accumulation and the risk for Parkinson's disease.NPJ Parkinsons Dis2023
36993627<i>MAPT</i> allele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson's disease risk and age at onset.medRxiv2023
36950378The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism.Cell Genom2023
37386035Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10.NPJ Parkinsons Dis2023
37409055Application of Aligned-UMAP to longitudinal biomedical studies.Patterns (N Y)2023
37467655MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset.Parkinsonism Relat Disord2023
37369645Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).NPJ Parkinsons Dis2023
37168844Variant biomarker discovery using mass spectrometry-based proteogenomics.Front Aging2023
37334620Parkinson's Disease Case Ascertainment in the Sister Study: A Cohort for Environmental Health Research.J Parkinsons Dis2023
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Collaborators

Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
Co-authored papers 186
Luigi Ferrucci
National Institute on Aging, National Institutes of Health
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Alexis Brice
Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS
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Nicholas W Wood
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Co-authored papers 51
Henry Houlden
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Co-authored papers 50
Stefania Bandinelli
Laboratory of Clinical Epidemiology
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Peter Heutink
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Andr?? G Uitterlinden
Erasmus University Medical Center
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Bruce M Psaty
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Pentti J Tienari
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Albert Hofman
Harvard T.H. Chan School of Public Health
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Tamara B Harris
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Cornelia M van Duijn
University of Oxford
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Alan B Zonderman
National Institute on Aging
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Yongmei Liu
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Jerome I Rotter
Co-authored papers 23
Valentina Escott-Price
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Mina Ryten
UCL Great Ormond Street Institute of Child Health, University College London
Co-authored papers 21
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 21
Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 20
John Q Trojanowski
University of Pennsylvania
Co-authored papers 20
Lenore J Launer
Co-authored papers 19
Vilmundur Gudnason
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Peter St George-Hyslop
Cambridge Institute for Medical Research, University of Cambridge
Co-authored papers 19
Timothy M Frayling
Co-authored papers 19
Michele K Evans
National Institute on Aging
Co-authored papers 18
Release 1.2